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Updated: Oct 2, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MiR-139-5p Inhibits the Development of Gastric Cancer through Targeting TPD52
Yuanbo Li1, Yan Sun2, Zhenlu Li1
1The Department of Emergency Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, China.
Background:
Many researchers have confirmed that miRNAs are involved in the pathogenesis of gastric cancer (GC). This study focused on investigating the specific functions of miR-139-5p in GC.
Methods:
MiR-139-5p and TPD52 expressions were observed by qRT-PCR or western blot in GC. The functional mechanism of miR-139-5p was explored by the luciferase reporter assay, transwell assay, and MTT assay.
Results:
MiR-139-5p downregulation and TPD52 upregulation were detected in GC. Adverse clinical features and prognosis in GC patients were related to low miR-139-5p expression. MiR-139-5p overexpression restrained GC cell proliferation and metastasis. Furthermore, miR-139-5p directly targeted TPD52. TPD52 silencing blocked GC progression. And TPD52 upregulation weakened the antitumor effect of miR-139-5p in GC.
Conclusion:
MiR-139-5p inhibits GC cell proliferation and metastasis through downregulating TPD52.
Insights
MicroRNA-139-5p (miR-139-5p) inhibits gastric cancer (GC) progression by downregulating TPD52. Low miR-139-5p expression correlates with poor prognosis in GC patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) play a role in gastric cancer (GC) development.
- This study investigates the specific role of miR-139-5p in GC pathogenesis.
Purpose of the Study:
- To elucidate the function of miR-139-5p in gastric cancer.
- To identify the molecular mechanism underlying miR-139-5p's action in GC.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and western blot were used to assess miR-139-5p and TPD52 expression.
- Functional assays including luciferase reporter, Transwell, and MTT assays were performed.
- TPD52 silencing and overexpression experiments were conducted.
Main Results:
- miR-139-5p was downregulated, while TPD52 was upregulated in GC tissues.
- Reduced miR-139-5p expression correlated with adverse clinical features and poor prognosis.
- Overexpression of miR-139-5p suppressed GC cell proliferation and metastasis.
- miR-139-5p directly targeted TPD52, and TPD52 silencing inhibited GC progression.
- TPD52 upregulation diminished the anti-tumor effects of miR-139-5p.
Conclusions:
- miR-139-5p functions as a tumor suppressor in gastric cancer.
- The miR-139-5p/TPD52 axis is a critical regulator of GC cell proliferation and metastasis.
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